Phenotypic manifestations between male and female children with CDKL5 mutations von Liang, Jao-Shwann, Huang, Hsin, Wang, Jinn-Shyan, Lu, Jyh-Feng

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Morphological and Molecular Defects in Human Three-Dimensional Retinal Organoid Model of X-Linked Juvenile Retinoschisis von Huang, Kang-Chieh, Wang, Mong-Lien, Chen, Shih-Jen, Kuo, Jean-Cheng, Wang, Won-Jing, Nhi Nguyen, Phan Nguyen, Wahlin, Karl J., Lu, Jyh-Feng, Tran, Audrey A., Shi, Michael, Chien, Yueh, Yarmishyn, Aliaksandr A., Tsai, Ping-Hsing, Yang, Tien-Chun, Jane, Wann-Neng, Chang, Chia-Ching, Peng, Chi-Hsien, Schlaeger, Thorsten M., Chiou, Shih-Hwa

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SCN2A mutation in an infant presenting with migrating focal seizures and infantile spasm responsive to a ketogenic diet von Su, Da-Jyun, Lu, Jyh-Feng, Lin, Li-Ju, Liang, Jao-Shwann, Hung, Kun-Long

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Induction of p53‐independent growth inhibition in lung carcinoma cell A549 by gypenosides von Liu, Jung‐Sen, Chiang, Tzu‐Hsuan, Wang, Jinn‐Shyan, Lin, Li‐Ju, Chao, Wei‐Chih, Inbaraj, Baskaran Stephen, Lu, Jyh‐Feng, Chen, Bing‐Huei

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Flavonoids from Gynostemma pentaphyllum exhibit differential induction of cell cycle arrest in H460 and A549 cancer cells von Tsui, Ko-Chung, Chiang, Tzu-Hsuan, Wang, Jinn-Shyan, Lin, Li-Ju, Chao, Wei-Chih, Chen, Bing-Huei, Lu, Jyh-Feng

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The therapeutic implication of a novel SCN2A mutation associated early-onset epileptic encephalopathy with Rett-like features von Liang, Jao-Shwann, Lin, Li-Ju, Yang, Ming-Tao, Wang, Jinn-Shyan, Lu, Jyh-Feng

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Tubulinopathy Presenting as Developmental and Epileptic Encephalopathy von Hung, Kun-Long, Lu, Jyh-Feng, Su, Da-Jyun, Hsu, Su-Jin, Wang, Lee-Chin

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Generation of induced pluripotent stem cells from a patient with X-linked juvenile retinoschisis von Peng, Chi-Hsien, Huang, Kang-Chieh, Lu, Huai-En, Syu, Shih-Han, Yarmishyn, Aliaksandr A., Lu, Jyh-Feng, Buddhakosai, Waradee, Lin, Tai-Chi, Hsu, Chih-Chien, Hwang, De-Kuang, Shen, Chia-Ning, Chen, Shih-Jen, Chiou, Shih-Hwa

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Novel PEX1 mutations in fibroblasts from children with Zellweger spectrum disorders exhibit temperature sensitive characteristics von Liang, Jao-Shwann, Hung, Kun-Long, Lin, Li-Ju, Ong, Winnie Peitee, Keng, Wee Teik, Lu, Jyh-Feng

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Mitochondrial DNA Content Varies with Pathological Characteristics of Breast Cancer von Bai, Ren-Kui, Chang, Julia, Yeh, Kun-Tu, Lou, Mary Ann, Lu, Jyh-Feng, Tan, Duan-Jun, Liu, Hao, Wong, Lee-Jun C.

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Probing water micro-solvation in proteins by water catalysed proton-transfer tautomerism von Shen, Jiun-Yi, Chao, Wei-Chih, Liu, Chun, Pan, Hsiao-An, Yang, Hsiao-Ching, Chen, Chi-Lin, Lan, Yi-Kang, Lin, Li-Ju, Wang, Jinn-Shyan, Lu, Jyh-Feng, Chun-Wei Chou, Steven, Tang, Kuo-Chun, Chou, Pi-Tai

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Antiproliferation Effect and Apoptosis Mechanism of Prostate Cancer Cell PC-3 by Flavonoids and Saponins Prepared from Gynostemma pentaphyllum von Cheng, Tse-Chou, Lu, Jyh-Feng, Wang, Jinn-Shyan, Lin, Li-Ju, Kuo, Hung-I, Chen, Bing-Huei

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Unveiling the structural features of nonnative trimers of human superoxide dismutase 1 von Chao, Wei-Chih, Lu, Jyh-Feng, Wang, Jinn-Shyan, Chiang, Tzu-Hsuan, Lin, Li-Ju, Lee, Yao-Lin, Chou, Pi-Tai

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Mutational Analyses on X-Linked Adrenoleukodystrophy Reveal a Novel Cryptic Splicing and Three Missense Mutations in the ABCD1 Gene von Hung, Kun-Long, MD, Wang, Jinn-Shyan, PhD, Keng, Wee Teik, MD, Chen, Hui-Ju, MD, Liang, Jao-Shwann, MD, Ngu, Lock Hock, MD, Lu, Jyh-Feng, PhD

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A Mouse Model for X-Linked Adrenoleukodystrophy von Lu, Jyh-Feng, Lawler, Ann M., Watkins, Paul A., Powers, James M., Moser, Ann B., Moser, Hugo W., Smith, Kirby D.

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A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy von Heinzer, Ann K., Watkins, Paul A., Lu, Jyh-Feng, Kemp, Stephan, Moser, Ann B., Li, Yuan Yuan, Mihalik, Stephanie, Powers, James M., Smith, Kirby D.

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Homology Modeling and Molecular Dynamics Simulation Combined with X‑ray Solution Scattering Defining Protein Structures of Thromboxane and Prostacyclin Synthases von Yang, Hsiao-Ching, Yang, Cheng-Han, Huang, Ming-Yi, Lu, Jyh-Feng, Wang, Jinn-Shyan, Yeh, Yi-Qi, Jeng, U-Ser

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Peroxisomal disorders with infantile seizures von Liang, Jao-Shwann, Lu, Jyh-Feng

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The role of peroxisomal ABC transporters in the mouse adrenal gland: the loss of Abcd2 (ALDR), Not Abcd1 (ALD), causes oxidative damage von Lu, Jyh-Feng, Barron-Casella, Emily, Deering, Rebecca, Heinzer, Ann K, Moser, Ann B, deMesy Bentley, Karen L, Wand, Gary S, C McGuinness, Martina, Pei, Zhengtong, Watkins, Paul A, Pujol, Aurora, Smith, Kirby D, Powers, James M

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Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens von Wu, Chien-Chih, Alper, Özgül M., Lu, Jyh-Feng, Wang, Song-Ping, Guo, Li, Chiang, Han-Sun, Wong, Lee-Jun C.

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